Visualizar Tese - Instituto de Biociências - Unesp

Visualizar Tese - Instituto de Biociências - Unesp Visualizar Tese - Instituto de Biociências - Unesp

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Cirilo, PDRREFERÊNCIAS225Penner AS, Rock MJ, Kielty CM et al. Microfibril-associated glycoprotein-2 interacts with fibrillin-1and fibrillin-2 suggesting a role for MAGP-2 in elastic fiber assembly. J Biol Chem, 277,35044-35049, 2002.Perez GD. Caracterização das deleções no cromossomo 7 em Leiomiomas Uterinos pelametodologia de hibridação in situ fluorescente. In: Dissertação de Mestrado, 81 pp, 2004.Perou CM, Sorlie T, Eisen MB et al. Molecular portraits of human breast tumours. Nature, 406, 747–752, 2000.Perou CM, Sorlie T, Eisen MB, et al. Molecular portraits of human breast tumours. Nature, 406, 747–752, 2000.Pinkel D, Segraves R, Sudar D et al: High resolution analysis of DNA copy number variation usingcomparative genomic hybridization to microarrays. Nat Genet, 20, 207–211, 1998.Pinto D, Marshall C, Feuk L et al. Copy-number variation in control population cohorts. Hum MolGenet, 16, 168–173, 2007.Pitt CW and Cooper JP. Pot1 inactivation leads to rampant telomere resection and loss in one cellcycle. Nucleic Acids Res, 38, 6968-6975, 2010.Pole JC, Courtay-Cahen C, Garcia MJ et al. High-resolution analysis of chromosome rearrangementson 8p in breast, colon and pancreatic cancer reveals a complex pattern of loss, gain andtranslocation. Oncogene, 25, 5693-5706, 2006.Polito P, Dal Cin P, Kazmierczak B et al. Deletion of HMG17 in uterine leiomyomas with ringchromosome 1. Cancer Genet Cytogenet, 108, 107-109, 1999.Pranzatelli, MR. The neurobiology of the opsoclonus-myoclonus syndrome. Clin. Neuropharmacol,15, 186–228, 1992.Prenzel KL, Schäfer E, Stippel D et al. Multiple giant leiomyomas of the esophagus and stomach. DisEsophagus, 19, 504-508, 2006.Przybytkowski E, Ferrario C, Basik M. The use of ultra-dense array CGH analysis for the discovery ofmicro-copy number alterations and gene fusions in the cancer genome. BMC Med Genomics,27; 4-6, 2011.Ptacek T, Song C, Walker CL et al. Physical mapping of distinct 7q22 deletions in uterine leiomyomaand analysis of a recently annotated 7q22 candidate gene. Cancer Genet Cytogenet, 174, 116-120, 2007.Quade BJ, Wang TY, Sornberger K et al. Molecular pathogenesis of uterine smooth muscle tumorsfrom transcriptional profiling. Genes Chrom Cancer, 40, 97–108, 2004.Quintana DG, Thome KC, Hou ZH et al. ORC5L, a new member of the human origin recognitioncomplex, is deleted in uterine leiomyomas and malignant myeloid diseases. J Biol Chem, 273,27137-27145, 1998.

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Cirilo, PDRREFERÊNCIAS225Penner AS, Rock MJ, Kielty CM et al. Microfibril-associated glycoprotein-2 interacts with fibrillin-1and fibrillin-2 suggesting a role for MAGP-2 in elastic fiber assembly. J Biol Chem, 277,35044-35049, 2002.Perez GD. Caracterização das <strong>de</strong>leções no cromossomo 7 em Leiomiomas Uterinos pelametodologia <strong>de</strong> hibridação in situ fluorescente. In: Dissertação <strong>de</strong> Mestrado, 81 pp, 2004.Perou CM, Sorlie T, Eisen MB et al. Molecular portraits of human breast tumours. Nature, 406, 747–752, 2000.Perou CM, Sorlie T, Eisen MB, et al. Molecular portraits of human breast tumours. Nature, 406, 747–752, 2000.Pinkel D, Segraves R, Sudar D et al: High resolution analysis of DNA copy number variation usingcomparative genomic hybridization to microarrays. Nat Genet, 20, 207–211, 1998.Pinto D, Marshall C, Feuk L et al. Copy-number variation in control population cohorts. Hum MolGenet, 16, 168–173, 2007.Pitt CW and Cooper JP. Pot1 inactivation leads to rampant telomere resection and loss in one cellcycle. Nucleic Acids Res, 38, 6968-6975, 2010.Pole JC, Courtay-Cahen C, Garcia MJ et al. High-resolution analysis of chromosome rearrangementson 8p in breast, colon and pancreatic cancer reveals a complex pattern of loss, gain andtranslocation. Oncogene, 25, 5693-5706, 2006.Polito P, Dal Cin P, Kazmierczak B et al. Deletion of HMG17 in uterine leiomyomas with ringchromosome 1. Cancer Genet Cytogenet, 108, 107-109, 1999.Pranzatelli, MR. The neurobiology of the opsoclonus-myoclonus syndrome. Clin. Neuropharmacol,15, 186–228, 1992.Prenzel KL, Schäfer E, Stippel D et al. Multiple giant leiomyomas of the esophagus and stomach. DisEsophagus, 19, 504-508, 2006.Przybytkowski E, Ferrario C, Basik M. The use of ultra-<strong>de</strong>nse array CGH analysis for the discovery ofmicro-copy number alterations and gene fusions in the cancer genome. BMC Med Genomics,27; 4-6, 2011.Ptacek T, Song C, Walker CL et al. Physical mapping of distinct 7q22 <strong>de</strong>letions in uterine leiomyomaand analysis of a recently annotated 7q22 candidate gene. Cancer Genet Cytogenet, 174, 116-120, 2007.Qua<strong>de</strong> BJ, Wang TY, Sornberger K et al. Molecular pathogenesis of uterine smooth muscle tumorsfrom transcriptional profiling. Genes Chrom Cancer, 40, 97–108, 2004.Quintana DG, Thome KC, Hou ZH et al. ORC5L, a new member of the human origin recognitioncomplex, is <strong>de</strong>leted in uterine leiomyomas and malignant myeloid diseases. J Biol Chem, 273,27137-27145, 1998.

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